HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94974531_94974532insGTA , CM000672.2:g.94974531_94974532insGTA | GRCh38 |
NC_000010.10:g.96734288_96734289insGTA , CM000672.1:g.96734288_96734289insGTA | GRCh37 |
NC_000010.9:g.96724278_96724279insGTA | NCBI36 |
NG_008385.1:g.40874_40875insGTA | |
NG_008385.2:g.41374_41375insGTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.961+2286_961+2287insGTA MANE Select | ENSP00000260682.6:n.961+2286_961+2287insGTA | |
ENST00000643112.1:c.820-6652_820-6651insGTA | ENSP00000496202.1:n.820-6652_820-6651insGTA | |
ENST00000260682.6:c.961+2286_961+2287insGTA | ENSP00000260682.6:n.961+2286_961+2287insGTA | |
NM_000771.3:c.961+2286_961+2287insGTA | NP_000762.2:n.961+2286_961+2287insGTA | |
NM_000771.4:c.961+2286_961+2287insGTA MANE Select | NP_000762.2:n.961+2286_961+2287insGTA |